Have questions? Visit https://www.reddit.com/r/SNPedia

rs61751263

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61751263(A;A)
Make rs61751263(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position94060760
GeneABCA4
is asnp
is mentioned by
dbSNPrs61751263
ebirs61751263
HLIrs61751263
Exacrs61751263
Varsomers61751263
Maprs61751263
PheGenIrs61751263
hapmaprs61751263
1000 genomesrs61751263
hgdprs61751263
ensemblrs61751263
gopubmedrs61751263
geneviewrs61751263
scholarrs61751263
googlers61751263
pharmgkbrs61751263
gwascentralrs61751263
openSNPrs61751263
23andMers61751263
23andMe allrs61751263
SNP Nexus

SNPshotrs61751263
SNPdbers61751263
MSV3drs61751263
GWAS Ctlgrs61751263
Max Magnitude0
ClinVar
Risk rs61751263(A;A)
Alt rs61751263(A;A)
Reference rs61751263(G;G)
Significance Pathogenic
Disease Stargardt disease 1 Retinitis pigmentosa 19 not provided
Variation info
Gene ABCA4
CLNDBN Stargardt disease 1 Retinitis pigmentosa 19 not provided
Reversed 1
HGVS NC_000001.10:g.94526316C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008351.3, RCV000008352.3, RCV000085450.1,